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血管生成
Tandutinib (MLN518)
品牌 | 厂商性质 | 产地 | 货期 |
---|---|---|---|
阿拉丁 | 生产商 | 上海 | 现货 |
产品参数
货号 | CAS号 | 操作 |
---|---|---|
T125150-100mg | 387867-13-2 | 询价 |
T125150-25mg | 387867-13-2 | 询价 |
T125150-500mg | 387867-13-2 | 询价 |
产品介绍
- 分子式 C31H42N6O4
- 分子量562.72
属性
熔点 | 172-183 °C |
溶解性 | Soluble in water (very poorly), DMSO (25 mg/ml, with slight warming), ethanol (25 mg/ml, with slight warming), and chloroform. |
存贮条件 | 储存温度-20°C |
描述
应用 | A piperazinyl quinazoline receptor tyrosine kinase inhibitor |
产品介绍 | Tandutinib (MLN518)是一种有效的FLT3拮抗剂,IC50为0.22 μM,同时也抑制PDGFR和c-Kit,对FLT3作用效果比CSF-1R强15到20倍,比FGFR, EGFR和KDR等强100倍以上 |
备注 | Tandutinib (MLN518, CT53518) is a potent FLT3 antagonist with IC50 of 0.22 μM, also inhibits PDGFR and c-Kit, 15 to 20-fold higher potency for FLT3 versus CSF-1R and >100-fold selectivity for the same target versus FGFR, EGFR and KDR. Phase |
生化机理 | Tandutinib is a piperazinyl quinazoline receptor tyrosine kinase inhibitor with antineoplastic activity. Tandutinib inhibits the autophosphorylation of Flt-3/Flk-2 (FMS-Like Tyrosine kinase-3), c-KIT and PDGF (platelet-derived growth factor) receptor tyrosine kinases, thereby inhibiting cellular proliferation and inducing apoptosis. Tandutinib is an inhibitor of PDGFR-beta. |
别名 | 坦度替尼; 4-[6-甲氧基-7-(3-哌啶-1-基丙氧基)喹唑啉-4-基]-N-(4-异丙基氧苯基)哌嗪-1-甲酰胺;MLN518; CT53518; MLN 518; CT 53518; MLN-518; CT-53518;4-[6-Methoxy-7-(3-piperidin-1-ylpropoxy)quinazolin-4-yl]-N-(4-propan-2-yloxyphenyl)piperazine-1-carboxamide; (4-(6-Methoxy-7-(3-piperidylpropoxy)quinazolin-4-yl)piperazinyl)-N-(4-(methylethoxy)phenyl)carboxamide |
Tandutinib (MLN518)信息由上海阿拉丁生化科技股份有限公司为您提供,如您想了解更多关于Tandutinib (MLN518)报价、型号、参数等信息,欢迎来电或留言咨询。
注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途